Sobhi Hamid Reza, Yamini Yadollah, Abadi Reza Haji Hosseini Baghdad
Department of Chemistry, Tehran University, P.O. Box 14155-6455, Tehran, Iran.
J Pharm Biomed Anal. 2007 Dec 21;45(5):769-74. doi: 10.1016/j.jpba.2007.09.026. Epub 2007 Sep 29.
In the present work, hollow fiber liquid phase microextraction (HF-LPME) in conjunction with reversed-phase HPLC/UV was developed for extraction and determination of trace amounts of chlorpromazine in biological fluids. The drug was extracted from an 11 ml aqueous sample (source phase; SP) into an organic phase impregnated in the pores of the hollow fiber (membrane phase; MP) followed by the back-extraction into a second aqueous solution (receiving phase; RP) located in the lumen of the hollow fiber. The effects of several factors such as the nature of organic solvent, compositions of SP and RP solutions, extraction time, ionic strength and stirring rate on the extraction efficiency of the drug were examined and optimized. Under the optimal conditions, enrichment factor of 250, dynamic linear range of 1-500 microgl(-1), and limit of detection of 0.5 microgl(-1) were obtained for the drug. The percent relative intra-day and inter-day standard deviation (R.S.D.%) based on three replicate determinations were 6.7 and 10.3%, respectively. The method was applied to drug level monitoring in the biological fluids and satisfactory results were obtained.
在本研究中,开发了中空纤维液相微萃取(HF-LPME)结合反相高效液相色谱/紫外检测法用于生物流体中痕量氯丙嗪的萃取和测定。药物从11毫升水样(源相;SP)萃取到浸渍于中空纤维孔隙中的有机相(膜相;MP),随后再反萃取到位于中空纤维内腔的第二种水溶液(接收相;RP)中。考察并优化了多种因素如有机溶剂的性质、源相和接收相溶液的组成、萃取时间、离子强度和搅拌速率对药物萃取效率的影响。在最佳条件下,该药物的富集因子为250,动态线性范围为1 - 500 μg l⁻¹,检测限为0.5 μg l⁻¹。基于三次重复测定的日内和日间相对标准偏差百分比(R.S.D.%)分别为6.7%和10.3%。该方法应用于生物流体中的药物水平监测,获得了满意的结果。